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rs1057516045

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057516045(C;T)
Make rs1057516045(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position225403404
GeneLBR
is asnp
is mentioned by
dbSNPrs1057516045
dbSNP (old)rs1057516045
ClinGenrs1057516045
ebirs1057516045
HLIrs1057516045
Exacrs1057516045
Gnomadrs1057516045
Varsomers1057516045
Maprs1057516045
PheGenIrs1057516045
Biobankrs1057516045
1000 genomesrs1057516045
hgdprs1057516045
ensemblrs1057516045
gopubmedrs1057516045
geneviewrs1057516045
scholarrs1057516045
googlers1057516045
pharmgkbrs1057516045
gwascentralrs1057516045
openSNPrs1057516045
23andMers1057516045
23andMe allrs1057516045
SNPshotrs1057516045
SNPdbers1057516045
MSV3drs1057516045
GWAS Ctlgrs1057516045
Max Magnitude0
ClinVar
Risk rs1057516045(T;T)
Alt rs1057516045(T;T)
Reference Rs1057516045(C;C)
Significance Probable-Pathogenic
Disease Pelger-Huët anomaly
Variation info
Gene LBR
CLNDBN Pelger-Huët anomaly
Reversed 1
HGVS NC_000001.10:g.225591106G>A
CLNSRC
CLNACC RCV000408612.1,